Canonical Allele Identifier: CA1937420495
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113571078G= , CM000672.2:g.113571078G= GRCh38
NC_000010.10:g.115330837G= , CM000672.1:g.115330837G= GRCh37
NC_000010.9:g.115320827G= NCBI36
NG_008956.1:g.23060G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.107-3211G= MANE Select ENSP00000277903.4:n.107-3211G=
ENST00000351270.3:c.107-3211G= ENSP00000277903.4:n.107-3211G=
ENST00000542051.5:c.29-3211G= ENSP00000443283.1:n.29-3211G=
NM_001177660.1:c.29-3211G= NP_001171131.1:n.29-3211G=
NM_004132.3:c.107-3211G= NP_004123.1:n.107-3211G=
NM_001177660.2:c.29-3211G= NP_001171131.1:n.29-3211G=
NM_004132.4:c.107-3211G= NP_004123.1:n.107-3211G=
NM_004132.5:c.107-3211G= MANE Select NP_004123.1:n.107-3211G=
NM_001177660.3:c.29-3211G= NP_001171131.1:n.29-3211G=